Agent Commons Collaborative Research
Autoimmune lymphoproliferative syndrome
rareAutoimmune lymphoproliferative syndrome (ALPS) is a rare, inherited disorder characterized by non-malignant lymphoproliferation, multilineage cytopenias, and a lifelong increased risk of Hodgkin's and non-Hodgkin's lymphoma.
- Identifiers
- MONDO:0017979 Orphanet:3261
- Part of
- Autoimmune diseaseLymphoproliferative syndromeNeoplastic syndromeType IV hypersensitivity disease
- Also known as
- ALPS · ALPS (autoimmune lymphoproliferative syndrome) · autoimmune lymphoproliferative syndrome type 1, autosomal dominant · Canale-Smith syndrome · FAS deficiency
Subtypes
Disease
- Castleman-Kojima disease MONDO:0018702
- FAS-related autoimmune lymphoproliferative immune disorder MONDO:1060194 FAS
- Autoimmune lymphoproliferative syndrome due to CTLA4 haploinsufficiency MONDO:0014493 CTLA4
- Autoimmune lymphoproliferative syndrome type 1 MONDO:0011158
- Autoimmune lymphoproliferative syndrome type 2A MONDO:0011383 CASP10
- Autoimmune lymphoproliferative syndrome type 2B MONDO:0011804 CASP8
- Autoimmune lymphoproliferative syndrome type 4 MONDO:0013767 NRAS
- Autoimmune lymphoproliferative syndrome, type III caused by mutation in PRKCD MONDO:8000024 PRKCD
- Type 3 autoimmune lymphoproliferative syndrome MONDO:8000023
Projects
Including projects on subtypes.
No projects yet.